GVViZ
GVViZ visualizes disease-associated gene variants and transcript abundances from RNA-seq and next-generation sequencing data to integrate transcriptomics with gene–disease databases and generate heat maps and exportable tables for downstream analysis.
Key Features:
- RNA-seq-driven analysis: Handles RNA-seq-driven variable and complex gene–disease data annotation and expression analysis, producing dynamic heat map visualizations across large feature sets.
- Data integration: Integrates patient transcriptomics with public, proprietary, and in-house gene–disease databases to enable querying and exploration of gene annotation and classified disease phenotypes.
- Visualization capabilities: Visualizes complex datasets for chronic diseases and conditions and exports results as PNF/TIFF images and CSV text files containing gene names, Ensembl IDs, quantified abundances, expressed transcript lengths, and annotated diseases.
- Automated interactive visualization: Provides automated and interactive visualization functionality to support interpretation of transcriptomics data and gene expression patterns.
- High-throughput correlation analysis: Enables high-throughput correlations between patient diagnoses and transcriptomics data for comparative analyses.
Scientific Applications:
- Disease-focused transcriptomics visualization: Visualizes gene expression and variant-associated genes for conditions including Alzheimer's disease, arthritis, asthma, diabetes mellitus, heart failure, hypertension, obesity, osteoporosis, and multiple cancer disorders.
- Clinical correlation and biomarker discovery: Supports early detection of complex disorders and the development of personalized therapies by correlating clinical diagnoses with transcriptomics profiles.
- Gene expression dynamics and regulation: Facilitates study of gene expression dynamics and regulation using RNA-seq datasets.
Methodology:
Processes RNA-seq/next-generation sequencing data, integrates transcriptomics with gene–disease databases, generates dynamic heat map visualizations, supports querying/exploration of gene annotations and disease phenotypes, and exports image (PNF/TIFF) and table (CSV) outputs.
Topics
Details
- Cost:
- Free of charge
- Operating Systems:
- Mac, Linux, Windows
- Programming Languages:
- Java
- Added:
- 11/8/2021
- Last Updated:
- 11/8/2021
Operations
Publications
Ahmed Z, Renart EG, Zeeshan S, Dong X. Advancing clinical genomics and precision medicine with GVViZ: FAIR bioinformatics platform for variable gene-disease annotation, visualization, and expression analysis. Human Genomics. 2021;15(1). doi:10.1186/s40246-021-00336-1. PMID:34174938. PMCID:PMC8235866.